Characterization and In vitro Release & In vivo Behavior Study of Self-Assembled Nano-Emulsion in XiaoYao Pill for Enhanced Drug Delivery.

Guan QingXia, Zhu MeiWei, Wang LianZhi, Chen ZhongXin, Yang FangFang, Yang ZhiPing, Dai XiaoFang, Zhao Fang Yuan
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Abstract

Background: Traditional Chinese medicine formulations often contain hydrophobic components with limited solubility and stability, leading to low oral bioavailability. Self-assembled nanoparticles (SANs) have shown promise in enhancing oral bioavailability of these components. However, whether un-decocted Chinese herbal pellets can generate SANs and the impact of SANs formed by multiple components on pharmacokinetic parameters remains unexplored.

Methods: In this study, single-factor approach was employed to determine the optimal separation method of nano-emulsion phase of XiaoYao pill (N-XY). Morphological and particle size analyses confirmed the nanoscale nature of N-XY. High-performance liquid chromatography (HPLC) fingerprint analysis was conducted to compare the distribution of active ingredients among three different phases of XiaoYao pill (XY pill). In vitro release studies were performed to evaluate the release mechanism of four ingredients from N-XY. Additionally, in vivo pharmacokinetics and tissue distribution behaviors were investigated in rats.

Results: N-XY exhibited uniform and stable characteristics as a water-in-oil (O/W) nano-emulsion. Fingerprint analysis identified 25 characteristic peaks and 8 key ingredients in N-XY, with the highest peak areas. In vitro release studies showed a sustained release behavior of N-XY. The pharmacokinetics study showed that the ferulic acid of N-XY had a 1.37-fold higher AUC, 1.44-fold lower Vd/F, 1.39-fold lower CL/F, and a prolonged t1/2 than A-XY, indicating enhanced bioavailability due to reduced elimination. Furthermore, the tissue distribution revealed that the levels of paeoniflorin and ferulic acid from N-XY significantly increased in liver, spleen, lungs, uterus and ovaries, exhibiting targeting characteristics.

Conclusion: This study comprehensively explored the formation, characterization, and pharmacokinetics of nano-emulsion in XY pill, introducing novel perspectives and initiating preliminary research on potential SANs in un-decocted traditional Chinese medicine formulations. It also emphasized the importance of enhancing pharmacokinetics of hydrophobic components in Chinese herbal formulations and laid the foundation for future nano-formulation research for XY pill.

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小药丸中自组装纳米乳液的表征、体外释放和体内行为研究,用于增强给药效果。
背景:传统中药配方通常含有疏水性成分,其溶解性和稳定性有限,导致口服生物利用度较低。自组装纳米颗粒(SANs)有望提高这些成分的口服生物利用度。然而,未经煎煮的中药颗粒是否能生成 SANs,以及多种成分形成的 SANs 对药代动力学参数的影响仍有待探索:本研究采用单因素法确定了小儿消渴丸(N-XY)纳米乳相的最佳分离方法。形态和粒度分析证实了 N-XY 的纳米级性质。通过高效液相色谱(HPLC)指纹图谱分析,比较了小药丸(XY丸)有效成分在三种不同相中的分布。进行了体外释放研究,以评估 N-XY 中四种成分的释放机制。此外,还研究了大鼠体内药代动力学和组织分布行为:结果:N-XY作为一种油包水型(O/W)纳米乳液,表现出均匀稳定的特性。指纹图谱分析确定了 N-XY 中的 25 个特征峰和 8 种关键成分,其中峰面积最大。体外释放研究表明,N-XY 具有持续释放特性。药代动力学研究表明,与 A-XY 相比,N-XY 中阿魏酸的 AUC 高 1.37 倍,Vd/F 低 1.44 倍,CL/F 低 1.39 倍,t1/2 延长,这表明由于消除减少,生物利用度提高。此外,组织分布显示,N-XY中的芍药苷和阿魏酸在肝、脾、肺、子宫和卵巢中的含量显著增加,表现出靶向性特征:本研究全面探讨了XY丸中纳米乳剂的形成、表征和药代动力学,提出了新的观点,并启动了对未煎煮中药制剂中潜在SAN的初步研究。该研究还强调了在中药制剂中提高疏水性成分药代动力学的重要性,并为未来 XY 丸的纳米制剂研究奠定了基础。
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